Induction of Tryptophan Dioxygenase by Glucocorticoid Hormones

2 Induction of Tryptophan Dioxygenase by Glucocorticoid Hormones The de novo synthesis of tryptophan dioxygenase is induced by glucocorticoid hormones (cortisol in human beings and corticosterone in the rat). This is true induction of new mRNA and protein synthesis indeed. 

In isolated hepatocytes, after maximum induction of tryptophan dioxygenase by glucocorticoids, the uptake of tryptophan into the cells has a control coefficient of 0.75, whereas the control coefficient of tryptophan dioxygenase falls to 0.25. Therefore, the induction of tryptophan dioxygenase has only a limited effect on tryptophan catabolism and NAD synthesis (Salter and Pogson, 1985 Salter et al., 1986). In isolated perfused liver, although cortisol leads to a several-fold increase in tryptophan dioxygenase activity, there is only a relatively small increase in the rate of clearance of tryptophan from the perfusion medium (Kim and Miller, 1969). 

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The ability to metabolise a test dose of tryptophan has been widely adopted as a convenient and sensitive index of vitamin Bg nutritional status. However, induction of tryptophan dioxygenase by glucocorticoid hormones will result in a greater rate of formation of kynurenine and hydroxykynurenine than the capacity of kynureninase, and will thus lead to increased formation of kynurenic and xanthurenic acids—an effect similar to that seen in vitamin Bg deficiency. Such results may be erroneously interpreted as indicating vitamin Bg deficiency in a variety of subjects whose problem is increased glucocorticoid secretion as a result of stress or illness, not vitamin Bg deficiency. 

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